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Status |
Public on May 22, 2020 |
Title |
YFP-rep2 |
Sample type |
SRA |
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Source name |
Skeletal muscle
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Organism |
Mus musculus |
Characteristics |
strain: Pax7CreERT2/+; ROSA26YFP/+ cell type: Muscle stem cells treatment: PFA-perfused mice age: 7-month-old
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Extracted molecule |
polyA RNA |
Extraction protocol |
The fixed muscle stem cell isolation was following the isolation protocol of satellite cells, as described previously in Liu et al., 2015, except that Collagenase II for first digestion was used at 2000 U/mL.Cell suspension was sorted using a BD Influx cell sorter equipped with 405-nm, 488-nm, 561-nm and 633-nm lasers. The machine was carefully optimized for purity and viability. To get high quality RNA from fixed cells, the total RNA from fixed muscle stem cells were isolated using a miRNeasy FFPE Kit (Qiagen) following the protocol described in Thomsen et al., 2015. cDNA was generated following the SMART-Seq v4 Ultra Low Input RNA Kit for Sequencing (Clontech) protocol. The RNA-Seq libraries were sheared with a Covaris S220 and generated using Ovation Ultralow DR Multiplex System 9-16 (NuGEN Technologies). The libraries were sequenced using Illumina NextSeq 500 (2 x 75).
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina NextSeq 500 |
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Description |
freshly-isolated quiescent muscle stem cells from PFA-perfused Pax7CreERT2/+; ROSA26YFP/+ mice
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Data processing |
RNA-seq data were aligned using STAR (version 2.5.3a) with the parameters “–twopassMode Basic”, “–outFilterIntronMotifs RemoveNoncanonical”, “--outSAMstrandField intronMotif”, and “--outSAMmultNmax 1”. Then, StringTie (version 1.3.3) was used with the -e option to quantify gene expression levels according to the reference’s annotations. Furthermore, StringTie’s -b option was used so that output suitable for Ballgown (version 2.10.0) under R (version 3.4.1) could be produced. Genome_build: mm9 Supplementary_files_format_and_content: Table of genes by samples of FPKM values, as output by Ballgown. File format is tab-separated values (ASCII text file).
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Submission date |
Oct 03, 2018 |
Last update date |
May 22, 2020 |
Contact name |
Tom Cheung |
Organization name |
Hong Kong University of Science and Technology
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Department |
Division of Life Science
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Street address |
Clear Water Bay, Kowloon
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City |
Hong Kong |
ZIP/Postal code |
N/A |
Country |
Hong Kong |
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Platform ID |
GPL19057 |
Series (1) |
GSE120799 |
Transcriptome profiling of Dek over-expressed quiescent muscle stem cells in vivo |
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Relations |
BioSample |
SAMN10172577 |
SRA |
SRX4795041 |
Supplementary data files not provided |
SRA Run Selector |
Raw data are available in SRA |
Processed data are available on Series record |
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